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Key Documents

341274

Sigma-Aldrich

2-Methyl-2-vinyloxirane

95%

Synonym(s):

Isoprene monoxide

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About This Item

Empirical Formula (Hill Notation):
C5H8O
CAS Number:
Molecular Weight:
84.12
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

assay

95%

form

liquid

refractive index

n20/D 1.416 (lit.)

bp

80-81 °C (lit.)

density

0.857 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CC1(CO1)C=C

InChI

1S/C5H8O/c1-3-5(2)4-6-5/h3H,1,4H2,2H3

InChI key

FVCDMHWSPLRYAB-UHFFFAOYSA-N

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

17.6 °F - closed cup

flash_point_c

-8 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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J J Bogaards et al.
Chemico-biological interactions, 117(1), 1-14 (1999-04-06)
In the present study, the enzymatic conjugation of the isoprene monoepoxides 3,4 epoxy-3-methyl-1-butene (EPOX-I) and 3,4-epoxy-2-methyl-1-butene (EPOX-II) with glutathione was investigated, using purified glutathione S-transferases (GSTs) of the alpha, mu, pi and theta-class of rat and man. HPLC analysis of
Roberto Fabiani et al.
Mutation research, 629(1), 7-13 (2007-02-24)
Isoprene is produced in combustion processes and is widely used as an industrial chemical. It is a natural product emitted by plants and endogenously produced by humans and other mammals. Therefore, exposure to isoprene from both endogenous and exogenous sources
J J Bogaards et al.
Chemico-biological interactions, 138(3), 247-265 (2001-11-21)
The present study was designed to explain the differences in isoprene toxicity between mouse and rat based on the liver concentrations of the assumed toxic metabolite isoprene diepoxide. In addition, extrapolation to the human situation was attempted. For this purpose
J J Bogaards et al.
Chemico-biological interactions, 102(3), 169-182 (1996-12-20)
The metabolism of isoprene was investigated with microsomes derived from cell lines expressing human CYP1A1, CYP1A2, CYP2A6, CYP2B6, CYP2C9, CYP2D6, CYP2E1, or CYP3A4. The formation of epoxide metabolites was determined by gas chromatographic analysis. CYP2E1 showed the highest rates of

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